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US20060035798A1 - Non-aqueous water and oil repellent compositions for a durable hydrophobic textile - Google Patents

Non-aqueous water and oil repellent compositions for a durable hydrophobic textile Download PDF

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Publication number
US20060035798A1
US20060035798A1 US11/254,201 US25420105A US2006035798A1 US 20060035798 A1 US20060035798 A1 US 20060035798A1 US 25420105 A US25420105 A US 25420105A US 2006035798 A1 US2006035798 A1 US 2006035798A1
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United States
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sub
component
group
fluorine
oil repellent
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US11/254,201
Inventor
Larry Rising
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Individual
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Individual
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Priority claimed from US10/611,746 external-priority patent/US20040006827A1/en
Application filed by Individual filed Critical Individual
Priority to US11/254,201 priority Critical patent/US20060035798A1/en
Publication of US20060035798A1 publication Critical patent/US20060035798A1/en
Abandoned legal-status Critical Current

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Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/08Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with halogenated hydrocarbons
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06BTREATING TEXTILE MATERIALS USING LIQUIDS, GASES OR VAPOURS
    • D06B9/00Solvent-treatment of textile materials
    • D06B9/06Solvent-treatment of textile materials with recovery of the solvent
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/263Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
    • D06M15/277Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof containing fluorine
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M23/00Treatment of fibres, threads, yarns, fabrics or fibrous goods made from such materials, characterised by the process
    • D06M23/10Processes in which the treating agent is dissolved or dispersed in organic solvents; Processes for the recovery of organic solvents thereof
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/10Repellency against liquids
    • D06M2200/11Oleophobic properties
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/10Repellency against liquids
    • D06M2200/12Hydrophobic properties
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50Manufacturing or production processes characterised by the final manufactured product
    • Y02P70/62Manufacturing or production processes characterised by the final manufactured product related technologies for production or treatment of textile or flexible materials or products thereof, including footwear

Definitions

  • Fluoro-chemicals are now applied to substrates via application with water based (aqueous) carriers requiring other auxiliary chemicals i.e.: emulsifiers, de-foaming agents, wetting agents and dispersing agents to keep organics in suspension.
  • auxiliary chemicals i.e.: emulsifiers, de-foaming agents, wetting agents and dispersing agents to keep organics in suspension.
  • chlorinated hydrocarbons have been used in the past as carrier mediums to apply organic chemicals to substrates when an aqueous carrier could not be used. Most chlorinated hydrocarbons are being phased out by mandate of the Environmental Protection Agency (EPA).
  • EPA Environmental Protection Agency
  • Chlorofluorocarbons have been widely used as solvents for solvent-based fluorine-containing surface treatment compositions because the chlorofluorocarbons are less toxic, nonflammable and chemically stable.
  • Particularly CFC-113 which has a moderate boiling point, has been widely used.
  • ozone layer depletion by specific chlorofluorocarbons such as CFC-113 became a problem and production of such chlorofluorocarbons has been discontinued on a world-wide scale.
  • NPB n-propyl bromide
  • 2,3-dihydrodeca-fluoropentane have shown to be a excellent alternatives to current aqueous and chlorinated hydrocarbons as a carrier medium for application of organics to substrates. Both are examples of a non-regulated, non-toxic alternatives with little to no ozone pollution properties. NPB is very economical and environmentally friendly.
  • NPB NPB
  • the invention relates to non-aqueous surface treatments to provide substrates oil and water repellant.
  • the treatment of home textiles and apparel which achieve desired effects with significantly smaller amounts of expensive fluorocarbon compounds as compared to available current technology, illustrated in Example 2 Compared to Example 4.
  • compositions according to the invention should furthermore impart to the substrates, in particular the home textiles, water-repellant actions that meet increased requirements.
  • Another object comprises providing treatment compositions with which the heat treatment can be carried out at the lowest temperature or, preferably no heat treatment being necessary (Example 3).
  • invention relates to substrates from the group consisting of naturally occurring and synthetic textiles and their mixtures, leather, mineral substances, thermoplastic and thermosetting polymers and paper, which are treated with fluorine-containing compositions of the type mentioned below in an amount of 10 to 10,000 ppm, preferably 50 to 5,000 ppm, particularly preferably 100 to 2,000 ppm, calculated as fluorine and based on the total weight of substrates provided with an oil-, water- and soil-repellant treatment.
  • other textile auxiliary chemicals can be added during preparation of the treatment formula as according to the invention, or subsequently.
  • additives are crease-proofing and soft handle agents, melamine, flame retardant, oleophobizing agents, hydrophobizing agents, urethane, finishing agents, extenders and antimicrobials for textile auxiliaries and others.
  • Substrates which are suitable for imparting oil-, water- and soil-repellant properties according to the invention are: linen, cotton, wool, silk, jute, polyamide, polyester, polyacrylonitrile and mixtures thereof, leather, stone slabs, floor tiles, glazed tiles, roof tiles, glass, ground surfaces of silicon, foils and films and compact workpieces of polyolefins, polyesters, polyamides, polycarbonates, polyurethane, polyacetals, polyethers, polysulphides, polysulphones, polyamides and other thermoplastics, as well as of phenol/formaldehyde resins, urea/formaldehyde resins, melamine/formaldehyde resins and other thermosetting resins, paper and paper-like materials, such as paperboard.
  • Preferred base substrates are home textiles based on naturally occurring and synthetic textiles and their mixtures, which are employed, for example, as carpets, curtains, decorative materials or coverings for upholstered furniture.
  • compositions according to the invention are known to the expert and are, for example, foaming, dipping or spraying of the base substrates; the compositions according to the invention furthermore can be employed during the production of the base substrates, for example the pulp.
  • Textiles as base substrates, preferably home textiles and apparel can be treated, for example, in the padding, spraying or foaming process.
  • the padder consists of a liquor trough (chassis) and at least one pair of rubber rolls (Example 2).
  • the textiles to be treated are impregnated with the treatment liquor in the chassis and squeezed off between the rolls; the liquor runs back into the chassis. It is very important that a uniform liquor pick-up is achieved over the entire width of the goods during squeezing-off.
  • the liquor pick-up is stated in percentage of the weight of goods, and for normal textile constructions can be between 30 and 300%, depending on the quality of the goods and the padder pressure used.
  • the spraying process (Example 3) the textile is sprayed with the treatment liquor.
  • the treatment liquor is finely divided by nozzles and applied uniformly. An amount of treatment liquor precisely defined beforehand is applied to one square meter of textile goods.
  • the treatment liquor is continuously foamed mechanically in a commercially available mixer with out the addition of a foaming agent.
  • the foam is produced in the mixing head by mixing the liquor with air.
  • the foam, which emerges, is conveyed via a foam line to a discharge slot in the applicator.
  • the goods are pressed against the slot and taken off via a separate unit, for example a stenter frame.
  • a concentration of 98% NPB and 2% Perfluoroalkyl polyacrylate were used.
  • the experiments were carried out on the Gaston Systems, Inc. Foam Applicator, Stanly, N.C.
  • this invention involves the surprising discovery that the use of NPB applied in 100% concentration via dipping and squeezing with pressure rollers (Padding) and the NPB being evaporated away imparts a much improved softness and luster to textile substrates, especially home furnishing, apparel fabrics and upholstery fabrics.
  • the textiles preferably home textiles
  • the textiles are dried, it being possible to use temperatures of 120.degree. to 170.degree. C. to achieve the desired treatment effect according to the known procedure.
  • good oil-, water- and soil-repellant treatments can also be obtained with the new compositions according to the invention at significantly lower drying temperatures, for example at 25.degree. C. (Example 3).
  • Oil-repellency (according to AATCC 118-1972): The test sample is placed on a horizontal, smooth surface, a small drop (drop diameter about 5 mm) of he test liquids is applied to the test sample with the aid of a dropping pipette, In addition, the sample is evaluated as specified.
  • the AATCC oil-repellency level of a test fabric is the highest number of that test liquid which does not wet or penetrate into the test material within a time span of 30 seconds.
  • the test liquids and mixtures for the test method are: No. 1: Nujol or paraffin oil DAB 8; No. 2: 65% by volume of Nujol and 35% by volume of n-hexadecane; No. 3: n-hexadecane; No. 4: n-tetradecane; No. 5: n-dodecane; No. 6: n-decane; No. 7: n-octane; No. 8: n-heptane.
  • Repellency towards a water/alcohol mixture (hydrophobicity): Drops of water/isopropanol mixtures (ratio 90/10 to 10/90) are applied to the test sample.
  • the test result corresponds to the mixture with the highest isopropanol content which remains on the test sample in unchanged form for at least 20 seconds (the value 80/20, for example, is better than 20/80).
  • compositions which are not according to the invention (Example 4) and which represent the prior art are the following: Nuva HPU (Clariant Corporation). Scotchgard.RTM. FC 396 (3M Comp.) according to DE-A 2 149 292 Baygard.RTM. SF-A. (Bayer AG) according to DE-A 3 307 420 and Zonyl (E.I. Dupont)
  • compositions according to the invention are non-aqueous solutions contents of which comprise a mixture of NPB or 2,3-dihydrodeca-fluoropentane (component A) and one or more poly (meth) acrylates (component B).
  • the substrates used were (1) White Polyester 8 oz/sq yd (PES), (2) 100% Cotton interlock and (3) 60/40 PES and Rayon Blend.

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Dispersion Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

The object of the invention is to provide a fluorine-containing non-aqueous surface treatment composition for application by current commercially available equipment that has, excellent performance, a long shelf life, reduced energy consumption, very little to no ozone layer depletion and global warming. and is highly safe due to the non-flammability or flame retardant characteristics.

Description

  • This application is a continuation in part of patent application Ser. No. 10/611,746, Filed Jun. 30, 2003, Titled “Chemical formulations and methods utilizing NPB (n-propyl bromide) as non-aqueous carrier mediums to apply fluorocarbons and other organic chemicals to substrates”
  • BACKGROUND OF THE INVENTION
  • Fluoro-chemicals are now applied to substrates via application with water based (aqueous) carriers requiring other auxiliary chemicals i.e.: emulsifiers, de-foaming agents, wetting agents and dispersing agents to keep organics in suspension.
  • These auxiliary chemicals needed for aqueous application often lesson the intended benefit of the applied chemical to the substrate. Aqueous chemistries require high curing temperatures and expensive drying systems to evaporate the water. Chlorinated hydrocarbons have been used in the past as carrier mediums to apply organic chemicals to substrates when an aqueous carrier could not be used. Most chlorinated hydrocarbons are being phased out by mandate of the Environmental Protection Agency (EPA).
  • Chlorofluorocarbons have been widely used as solvents for solvent-based fluorine-containing surface treatment compositions because the chlorofluorocarbons are less toxic, nonflammable and chemically stable. Particularly CFC-113, which has a moderate boiling point, has been widely used. However, ozone layer depletion by specific chlorofluorocarbons such as CFC-113 became a problem and production of such chlorofluorocarbons has been discontinued on a world-wide scale.
  • BRIEF SUMMERY OF THE INVENTION
  • By this invention, NPB (n-propyl bromide) and 2,3-dihydrodeca-fluoropentane have shown to be a excellent alternatives to current aqueous and chlorinated hydrocarbons as a carrier medium for application of organics to substrates. Both are examples of a non-regulated, non-toxic alternatives with little to no ozone pollution properties. NPB is very economical and environmentally friendly.
  • After extensive study, it has been found that the use of NPB as a carrier for application dramatically improves the performances and durability of textiles and that this invention is superior to current methods and chemistry being applied by foam.
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • The invention relates to non-aqueous surface treatments to provide substrates oil and water repellant. As example, the treatment of home textiles and apparel, which achieve desired effects with significantly smaller amounts of expensive fluorocarbon compounds as compared to available current technology, illustrated in Example 2 Compared to Example 4.
  • The following description, taken in conjunction with the referenced examples, is presented to enable one of ordinary skill in the art to make and use the invention. Various modifications will be readily apparent to those Skilled in the art, and the general principles defined herein may be applied to a wide range of aspects. Thus, the present invention is not intended to be limited to the aspects presented, but is to be accorded the widest scope consistent with the principles and novel features disclosed herein. Furthermore, the compositions according to the invention should furthermore impart to the substrates, in particular the home textiles, water-repellant actions that meet increased requirements.
  • Another object comprises providing treatment compositions with which the heat treatment can be carried out at the lowest temperature or, preferably no heat treatment being necessary (Example 3).
  • In one aspect, invention relates to substrates from the group consisting of naturally occurring and synthetic textiles and their mixtures, leather, mineral substances, thermoplastic and thermosetting polymers and paper, which are treated with fluorine-containing compositions of the type mentioned below in an amount of 10 to 10,000 ppm, preferably 50 to 5,000 ppm, particularly preferably 100 to 2,000 ppm, calculated as fluorine and based on the total weight of substrates provided with an oil-, water- and soil-repellant treatment. In another aspect, other textile auxiliary chemicals can be added during preparation of the treatment formula as according to the invention, or subsequently. Such additives are crease-proofing and soft handle agents, melamine, flame retardant, oleophobizing agents, hydrophobizing agents, urethane, finishing agents, extenders and antimicrobials for textile auxiliaries and others.
  • Substrates which are suitable for imparting oil-, water- and soil-repellant properties according to the invention are: linen, cotton, wool, silk, jute, polyamide, polyester, polyacrylonitrile and mixtures thereof, leather, stone slabs, floor tiles, glazed tiles, roof tiles, glass, ground surfaces of silicon, foils and films and compact workpieces of polyolefins, polyesters, polyamides, polycarbonates, polyurethane, polyacetals, polyethers, polysulphides, polysulphones, polyamides and other thermoplastics, as well as of phenol/formaldehyde resins, urea/formaldehyde resins, melamine/formaldehyde resins and other thermosetting resins, paper and paper-like materials, such as paperboard. Preferred base substrates are home textiles based on naturally occurring and synthetic textiles and their mixtures, which are employed, for example, as carpets, curtains, decorative materials or coverings for upholstered furniture.
  • Processes for the treatment of such base substrates and therefore for application of the fluorine-containing compositions according to the invention are known to the expert and are, for example, foaming, dipping or spraying of the base substrates; the compositions according to the invention furthermore can be employed during the production of the base substrates, for example the pulp.
  • Textiles as base substrates, preferably home textiles and apparel can be treated, for example, in the padding, spraying or foaming process. The padder consists of a liquor trough (chassis) and at least one pair of rubber rolls (Example 2). The textiles to be treated are impregnated with the treatment liquor in the chassis and squeezed off between the rolls; the liquor runs back into the chassis. It is very important that a uniform liquor pick-up is achieved over the entire width of the goods during squeezing-off. In the padding process, the liquor pick-up is stated in percentage of the weight of goods, and for normal textile constructions can be between 30 and 300%, depending on the quality of the goods and the padder pressure used. In the spraying process, (Example 3) the textile is sprayed with the treatment liquor. The treatment liquor is finely divided by nozzles and applied uniformly. An amount of treatment liquor precisely defined beforehand is applied to one square meter of textile goods.
  • In the foaming process, the treatment liquor is continuously foamed mechanically in a commercially available mixer with out the addition of a foaming agent. The foam is produced in the mixing head by mixing the liquor with air. The foam, which emerges, is conveyed via a foam line to a discharge slot in the applicator. The goods are pressed against the slot and taken off via a separate unit, for example a stenter frame. In example 1, a concentration of 98% NPB and 2% Perfluoroalkyl polyacrylate were used. The experiments were carried out on the Gaston Systems, Inc. Foam Applicator, Stanly, N.C.
  • By the invention, it has been discovered surprisingly that mixtures of NPB and Perfluoroalkyl polyacrylate can be foamed with or without the aid of a foaming agent (Example 1). Not using foaming agents greatly improves the benefit of the applied fluorine composition to the substrate and reduces the amount of compound added to fabric to achieve water and oil repellency. In another aspect, this invention involves the surprising discovery that the use of NPB applied in 100% concentration via dipping and squeezing with pressure rollers (Padding) and the NPB being evaporated away imparts a much improved softness and luster to textile substrates, especially home furnishing, apparel fabrics and upholstery fabrics.
  • After the treatment, the textiles, preferably home textiles, are dried, it being possible to use temperatures of 120.degree. to 170.degree. C. to achieve the desired treatment effect according to the known procedure. However, good oil-, water- and soil-repellant treatments can also be obtained with the new compositions according to the invention at significantly lower drying temperatures, for example at 25.degree. C. (Example 3).
  • Samples of the materials thus pretreated were taken for testing of the following effects:
  • Oil-repellency (according to AATCC 118-1972): The test sample is placed on a horizontal, smooth surface, a small drop (drop diameter about 5 mm) of he test liquids is applied to the test sample with the aid of a dropping pipette, In addition, the sample is evaluated as specified.
  • The AATCC oil-repellency level of a test fabric is the highest number of that test liquid which does not wet or penetrate into the test material within a time span of 30 seconds. The test liquids and mixtures for the test method are: No. 1: Nujol or paraffin oil DAB 8; No. 2: 65% by volume of Nujol and 35% by volume of n-hexadecane; No. 3: n-hexadecane; No. 4: n-tetradecane; No. 5: n-dodecane; No. 6: n-decane; No. 7: n-octane; No. 8: n-heptane.
  • Repellency towards a water/alcohol mixture (hydrophobicity): Drops of water/isopropanol mixtures (ratio 90/10 to 10/90) are applied to the test sample. The test result corresponds to the mixture with the highest isopropanol content which remains on the test sample in unchanged form for at least 20 seconds (the value 80/20, for example, is better than 20/80).
  • EXAMPLES
  • Compositions which are not according to the invention (Example 4) and which represent the prior art are the following: Nuva HPU (Clariant Corporation). Scotchgard.RTM. FC 396 (3M Comp.) according to DE-A 2 149 292 Baygard.RTM. SF-A. (Bayer AG) according to DE-A 3 307 420 and Zonyl (E.I. Dupont)
  • The compositions according to the invention (Examples 1, 2 & 3) are non-aqueous solutions contents of which comprise a mixture of NPB or 2,3-dihydrodeca-fluoropentane (component A) and one or more poly (meth) acrylates (component B).
  • Use of the Compositions According to the Invention Example 1
  • A solution of 98% NPB and 2% Perfluoroalkyl polyacrylate were mixed and applied to the foam generator which imparts the solution to a high speed mixer that generates the solution into foam. The foam was then dispensed to the substrates listed in below via an applicator at 30%-wet pickup. The substrates were then dried at 170 deg C. for 1-minute dwell time with the following results:
    Initial After 10 Home Laundries
    Example 1 Oil IPA Spray Fluoride Oil IPA Spray Fluoride
    Cotton 5 85 100 2160 ppm 2 60 70 1600 ppm
    Polyester 6 90 100 1170 ppm 5 90 90  980 ppm
    Pes/Rayon 6 80 100 5 60 70
  • Example 2
  • A solution of 99.6% NPB and 0.4% Perfluoroalkyl polyacrylate were mixed and applied to the substrates listed below via a pad applicator at 3.5 bars pressure. The solution was applied at noted wet pickup. Again, the substrates were dried at 170 deg C. with a 1-minute dwell.
    Initial After 10 Home Laundries
    Example 2 Oil IPA Spray Fluoride Oil IPA Spray Fluoride
    Cotton 6 100 100 2480 ppm 3 90 80 2200 ppm
    Polyester 8 90 100 1270 ppm 6 90 90 1100 ppm
    Pes/Rayon 8 80 100 6 8O 80
  • Example 3
  • A solution of 99.6% 2,3-dihydrodeca-fluoropentane and 0.4% Perfluoroalkyl polyacrylate were mixed and applied to the substrates listed below via a Spray at 1.5 bars pressure. The solution was applied at noted wet pickup. The substrates were air dried at room temperature.
    Initial After 10 Home Laundries
    Example 3 Oil IPA Spray Fluoride Oil IPA Spray Fluoride
    Cotton 6 85 100 2260 ppm 2 4O 60 1370 ppm
    Polyester 7 90 10O 1170 ppm 3 90 70 1080 ppm
    Pes/Rayon 6 80 100 3 60 60
  • Example 4 Use of the Compositions not According to the Invention
  • An aqueous Perfluoroalkyl polyacrylate dispersion using Nuva HPU at 2% concentration was prepared and applied via a padding applicator at 3.5 bars pressure. The solution was applied at noted wet pickup. Again, the substrates were dried at 170 deg C. with a 1-minute dwell.
    Initial After 10 Home Laundries
    Example 4 Oil IPA Spray Fluoride Oil IPA Spray Fluoride
    Cotton 7 100 100 2460 7 90 80 2210
    ppm ppm
    Polyester 6 60 100 1270 4-5 45-50 90 1100
    ppm ppm
    Pes/Rayon 5 60 100 2 35-40 70
  • In all examples, the substrates used were (1) White Polyester 8 oz/sq yd (PES), (2) 100% Cotton interlock and (3) 60/40 PES and Rayon Blend.

Claims (13)

1. A non-aqueous water and oil repellent composition for a durable hydrophobic textile comprising:
(A) a fluorine-containing polymer or copolymer component,
(B) a solvent component,
(C) a cross-linking or extender component.
2. A Water and oil repellent composition according to claim 1, wherein the fluorine containing component (A) is a surface treatment component and comprises at least one species selected from the group consisting of: (1) phosphorus-containing compounds having at least one fluorine-containing group selected from the group consisting of polyfluoroalkyl groups and polyfluoroalkenyl groups; (2) highly fluorinated organic compounds; and (3) polymers prepared using, as a monomer component, a compound having a at least one fluorine-containing group selected from the group consisting of polyfluoroalkyl groups and polyfluoroalkenyl groups, said highly fluorinated organic compound (2) being at least one compound selected from the group consisting of:
(A) at least one fluoroalkane selected from the group consisting of (CF.sub.3).sub.2 CF(CF.sub.2).sub.4 CF(CF.sub.3).sub.2 and ##STR36##
(B) at least one fluorochloro polyether selected from the group consisting of: F(CHClCF.sub.2 CF.sub.2 O).sub.n CHClCF.sub.3 (n is 5 on an average); F(CCl.sub.2 CF.sub.2 CF.sub.2 O).sub.n CCl.sub.2 CF.sub.3 (n is 5 on an average); F(CCl.sub.2 CF.sub.2 CF.sub.2 O). sub.n CCl.sub.2 CF.sub.2 Cl (n is 25 on an average); CCl.sub.2 FCF.sub.2 CF.sub.2 OCCl.sub.2 CF.sub.2 CF.sub.2 OCCl.sub.2 CF.sub.3; F(CCl.sub.x F.sub.y CF.sub.2 CF.sub.2 O).sub.n CCl.sub.x F.sub.y CF.sub.3 (n is 5 on an average), x+y=2, x:y=1:4); F(CF.sub.2 CF.sub.2 CF.sub.2 O).sub.x (CClFCF.sub.2 CF.sub.2 O).sub.y —CF.sub.2 CF.sub.2 COF (x+y is 20 on an average, x:y=2:1, x number of units and y number of units are arranged in a random order); and F(CF.sub.2 CF.sub.2 CF.sub.2 O).sub.x (CClFCF.sub.2 CF.sub.2 O).sub.y CF.sub.2 CF.sub.3 (x+y is 20 on an average, x:y=2:1, x number of units and y number of units are arranged in a random order), and
(C) fluorochloroolefin telomers whose main portion, defined as a portion except for terminal groups, is composed of repeating units of —CF.sub.2 CFCl—, the total of the repeating units of chlorotrifluoroethane in terms of degree of telomerization being 3 to 20, and said polymer (3) prepared using as, a monomer component, a compound having at least one fluorine-containing group selected from the group consisting of polyfluoroalkyl groups and polyfluoroalkenyl groups being at least one polymer selected from the group consisting of:
(A) a copolymer of at least one fluorine-containing monomer selected from the group consisting of polyfluoroalkyl-containing (meth)acrylic esters, polyfluoroalkenyl-containing (meth)acrylic esters, polyfluoroalkyl-containing vinyl compounds and poly-fluoroalkenyl-containing vinyl compounds, and another monomer copolymerizable therewith, the proportion of the fluorine-containing monomer being 20-95 parts by weight, based on 100 parts by weight of the total monomer component, and
(B) a polymer of at least one fluorine-containing monomer selected from the group consisting of polyfluoroalkyl-containing epoxy monomers and polyfluoroalkenyl-containing epoxy monomers, or a copolymer of the fluorine-containing monomer and another monomer copolymerizable therewith, the proportion of the fluorine-containing monomer being 20-100 parts by weight, based on 100 parts by weight of the total monomer component.
3. A Water and oil repellent composition according to claim 1, wherein the fluorine containing component (A) is a surface treatment component comprising a polymer prepared using as a monomer component having at least one fluorine-containing group selected from the group consisting of polyfluoroalkyl groups and polyfluoroalkenyl groups.
4. A Water and oil repellent composition according to claim 1, wherein the solvent component (B) is stabilized. wherein said stabilizer (or corrosion inhibitor) is selected from the group consisting of alkanols having 4 to 7 carbon atoms, nitroalkanes having 1 to 3 carbon atoms, 1,2-epoxyalkanes having 2 to 7 carbon atoms, acetylene alcohols having 3 to 9 carbon atoms, phosphite esters having 12 to 30 carbon atoms, ethers having 3 to 6 carbon atoms, unsaturated hydrocarbon compounds having 4 to 7 carbon atoms, triazoles, acetals having 4 to 7 carbon atoms, ketones having 3 to 5 carbon atoms, amines having 6 to 8 carbon atoms, and mixtures thereof.
5. A Water and oil repellent composition according to claim 1, wherein the solvent component (B) is a bromine-containing solvent and is a C.sub. 1-3 alogenated hydrocarbon having at least one bromine atom.
6. A water and oil repellent composition according to claim 1, wherein the solvent component (B) is a bromine-containing solvent with at least one compound selected from the group consisting of 1-bromopropane, 2-bromopropane and 1,2-dibromopropane
7. A Water and oil repellent composition according to claim 1, wherein the solvent component (B) is selected from the group consisting of: 2,3-dihydrodeca-fluoropentane, mixture of 2,3-dihydrodeca-fluoropentane and trans-1,2-dichloroethylene, mixture of 2,3-dihydrodeca-fluoropentane and trans-1,2-dichloroethylene with cyclopentane.
8. A Water and oil repellent composition according to claim 1, wherein the cross-linking or extender component (C), is selected from the group comprising one or more of the following: melamine formaldehyde derivatives, trimethylolmelamine, hexamethylolmelamine, epoxides, anhydrides and derivatives thereof.
Derivatives of isocyanates, diisocyanates. Polymers containing two or more blocked isocyanate compounds or aromatic blocked isocyanates. Monomers or polymers containing isocyanate compounds, zirconium tetra-butanolate, paraffine waxes, microcrystalline or semicrystalline waxes and melamine-paraffin waxes, whereas said component (C) is 0.001% to 60% by weight of component B.
9. A Water and oil repellent composition according to claim 1, which further contains (D), which is an antibacterial component comprising one or more organic antimicrobial agents to include: Silver containing resins, silver containing zeolites, silver containing glass, silver based ion exchange compounds, triclosan and inorganic antimicrobial materials: metal based zeolites, metal salts, metal oxides, metal hydroxides, transition metal ions, zinc oxide, pyrithione containing materials, tributyl oxides derivatives, 3-iodo-2 propyl butyl carbamate, n-butyl-1,2 benzisothiazoline, 10,10′-oxybisphenoxi arsine, sodium o-phenylphenate, whereby component (D) is 0.001% to 5% by weight of component (A).
10. A process for surface treatment of an article to be treated, which comprises treating the textile with the surface treatment compositions according to claim 1, followed by drying and curing.
11. A process for surface treatment of an article to be treated, which comprises treating the textile with the surface treatment compositions according to claim 9, followed by drying and curing.
12. A textile which is treated with the water and oil repellent compositions according to claim 1.
13. A textile which is treated with the compositions according to claim 9.
US11/254,201 2003-06-30 2005-10-20 Non-aqueous water and oil repellent compositions for a durable hydrophobic textile Abandoned US20060035798A1 (en)

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US7842625B1 (en) 2006-10-26 2010-11-30 Nano-Tex, Inc. Methods for treating fabric to facilitate moisture transfer from one side to the other

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US3657173A (en) * 1969-03-03 1972-04-18 Du Pont Oil and water repellent compositions
US6120892A (en) * 1997-11-20 2000-09-19 E. I. Du Pont De Nemours And Company Waterborne fluoropolymer solutions for treating hard surfaces
US20030224112A1 (en) * 2002-06-03 2003-12-04 3M Innovative Properties Company Fluorochemical composition and method of treatment of a substrate therewith to render substrate oil-and/or water repellent
US7435774B2 (en) * 2002-09-11 2008-10-14 Peach State Labs, Inc. Fluoromonomers, fluoropolymers, methods of preparing them, and their application to various surfaces and substrates

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US3637614A (en) * 1969-02-27 1972-01-25 Du Pont Solvent soluble dry soil resistant fluoropolymers
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US20030224112A1 (en) * 2002-06-03 2003-12-04 3M Innovative Properties Company Fluorochemical composition and method of treatment of a substrate therewith to render substrate oil-and/or water repellent
US7435774B2 (en) * 2002-09-11 2008-10-14 Peach State Labs, Inc. Fluoromonomers, fluoropolymers, methods of preparing them, and their application to various surfaces and substrates

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US7842625B1 (en) 2006-10-26 2010-11-30 Nano-Tex, Inc. Methods for treating fabric to facilitate moisture transfer from one side to the other

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